Cas no 38209-58-4 (Methyl 2-(3,4-dimethoxyphenyl)-2-oxoacetate)
Methyl 2-(3,4-dimethoxyphenyl)-2-oxoacetate Chemical and Physical Properties
Names and Identifiers
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- methyl 2-(3,4-dimethoxyphenyl)-2-oxoacetate
- CTK6I6913
- methyl (3,4-dimethoxyphenyl)(oxo)acetate
- AG-C-11882
- AC1LVUYP
- (3,4-Dimethoxy-phenyl)-glyoxylsaeure-methylester
- methyl 3,4-dimethoxybenzoylformate
- Veratroylameisensaeure-methylester
- 3,4-Dimethoxy-benzoylameisensaeuremethylester
- 3,4-Dimethoxy-phenylglyoxylsaeure-methylester
- (3,4-dimethoxy-phenyl)-glyoxylic acid methyl ester
- SBB096626
- 3-(3,4-DIMETHOXYPHENYL)-3-OXO-PROPIONIC ACIDMETHYL ESTER
- 3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester
- AB-131
- Benzeneacetic acid, 3,4-dimethoxy-.alpha.-oxo-, methyl ester
- SCHEMBL13890438
- DTXSID0068078
- 38209-58-4
- Benzeneacetic acid, 3,4-dimethoxy-alpha-oxo-, methyl ester
- methyl2-(3,4-dimethoxyphenyl)-2-oxoacetate
- RRANFHUAXGKYBS-UHFFFAOYSA-N
- 3,4-Dimethoxy-alpha-oxobenzeneacetic acid methyl ester
- BS-47840
- DB-086983
- F73857
- Methyl 3,4-dimethoxybenzoylacetate
- AB-131/42301228
- Methyl 2-(3,4-dimethoxyphenyl)-2-oxoacetate
-
- Inchi: 1S/C11H12O5/c1-14-8-5-4-7(6-9(8)15-2)10(12)11(13)16-3/h4-6H,1-3H3
- InChI Key: RRANFHUAXGKYBS-UHFFFAOYSA-N
- SMILES: O(C)C1C=C(C(C(=O)OC)=O)C=CC=1OC
Computed Properties
- Exact Mass: 238.08400
- Monoisotopic Mass: 224.06847348g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 16
- Rotatable Bond Count: 5
- Complexity: 263
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 1.8
- Topological Polar Surface Area: 61.8?2
Experimental Properties
- PSA: 61.83000
- LogP: 1.44960
Methyl 2-(3,4-dimethoxyphenyl)-2-oxoacetate Customs Data
- HS CODE:2918990090
- Customs Data:
China Customs Code:
2918990090Overview:
2918990090. Other additional oxy carboxylic acids(Including anhydrides\Acyl halide\Peroxides, peroxyacids and derivatives of this tax number). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Methyl 2-(3,4-dimethoxyphenyl)-2-oxoacetate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 014808-1g |
3-(3,4-Dimethoxyphenyl)-3-oxo-propionic acidmethyl ester |
38209-58-4 | 1g |
£370.00 | 2022-03-01 | ||
| 1PlusChem | 1P00C8NY-100mg |
3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester |
38209-58-4 | 98% | 100mg |
$29.00 | 2023-12-17 | |
| 1PlusChem | 1P00C8NY-250mg |
3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester |
38209-58-4 | 98% | 250mg |
$40.00 | 2023-12-17 | |
| 1PlusChem | 1P00C8NY-1g |
3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester |
38209-58-4 | 95% | 1g |
$118.00 | 2024-05-03 | |
| 1PlusChem | 1P00C8NY-5g |
3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester |
38209-58-4 | 98% | 5g |
$316.00 | 2023-12-17 | |
| Aaron | AR00C8WA-100mg |
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38209-58-4 | 98% | 100mg |
$8.00 | 2025-02-12 | |
| Aaron | AR00C8WA-250mg |
3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester |
38209-58-4 | 98% | 250mg |
$18.00 | 2025-02-12 | |
| Aaron | AR00C8WA-1g |
3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester |
38209-58-4 | 97% | 1g |
$70.00 | 2025-04-02 | |
| Aaron | AR00C8WA-5g |
3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester |
38209-58-4 | 97% | 5g |
$263.00 | 2025-03-07 | |
| A2B Chem LLC | AF70302-100mg |
3,4-Dimethoxy-α-oxobenzeneacetic acid methyl ester |
38209-58-4 | 97% | 100mg |
$8.00 | 2023-12-30 |
Methyl 2-(3,4-dimethoxyphenyl)-2-oxoacetate Related Literature
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Jonas Kind,Lukas Kaltschnee,Martin Leyendecker,Christina M. Thiele Chem. Commun., 2016,52, 12506-12509
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Goonay Yousefalizadeh,Shideh Ahmadi,Nicholas J. Mosey,Kevin G. Stamplecoskie Nanoscale, 2021,13, 242-252
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Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
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Veluru Jagadeesh babu,Sesha Vempati RSC Adv., 2015,5, 66367-66375
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Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
Additional information on Methyl 2-(3,4-dimethoxyphenyl)-2-oxoacetate
Comprehensive Overview of Methyl 2-(3,4-dimethoxyphenyl)-2-oxoacetate (CAS No. 38209-58-4)
Methyl 2-(3,4-dimethoxyphenyl)-2-oxoacetate, with the CAS number 38209-58-4, is a specialized organic compound widely utilized in pharmaceutical and agrochemical research. This ester derivative, featuring a dimethoxyphenyl moiety, is pivotal in synthesizing intermediates for bioactive molecules. Its unique structure, combining an oxoacetate group with aromatic methoxy substitutions, makes it a versatile building block in medicinal chemistry. Researchers often explore its applications in drug discovery, particularly for designing antioxidant and neuroprotective agents, aligning with current trends in neurodegenerative disease research.
The compound’s chemical properties, such as solubility in organic solvents and stability under controlled conditions, enhance its utility in organic synthesis. Recent studies highlight its role in developing flavonoid analogs, a hot topic due to their potential in anti-inflammatory therapies. With growing interest in natural product derivatives, Methyl 2-(3,4-dimethoxyphenyl)-2-oxoacetate garners attention for mimicking plant-based bioactive structures. This aligns with the surge in searches for sustainable chemistry and green synthesis methods, as industries seek eco-friendly alternatives.
Analytical techniques like HPLC and NMR spectroscopy are critical for characterizing this compound, ensuring purity for high-yield reactions. Its CAS registry (38209-58-4) simplifies procurement for labs focusing on peptide coupling or heterocyclic compound development. Notably, its methoxy groups contribute to electron-rich aromatic systems, a feature exploited in photocatalysis research—a trending area in renewable energy applications.
In the context of user search trends, queries often revolve around "synthesis of dimethoxyphenyl derivatives" or "applications of oxoacetate esters," reflecting its niche yet expanding relevance. The compound’s compatibility with microwave-assisted synthesis (a popular lab technique) further boosts its appeal. Additionally, its potential in flavor and fragrance industries—owing to its aromatic profile—resonates with searches for "food-grade esters."
Regulatory-wise, Methyl 2-(3,4-dimethoxyphenyl)-2-oxoacetate is compliant with major safety standards when handled under GMP guidelines. This ensures its adoption in preclinical studies without restrictive hurdles. As AI-driven drug design gains traction, this compound’s structural data is increasingly mined for machine learning models predicting bioactivity—a synergy of chemistry and tech that dominates current scientific discourse.
To conclude, CAS 38209-58-4 exemplifies innovation at the intersection of traditional organic chemistry and cutting-edge research. Its adaptability across pharmaceuticals, agriculture, and material science underscores its enduring value. For researchers navigating structure-activity relationships or scalable synthesis, this compound remains a cornerstone in advancing small-molecule therapeutics.
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